Catalog Number

7031

Brand Name

PolyMem

Version/Model Number

PolyMem

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KMF

Product Code Name

Bandage, Liquid

Public Device Record Key

f1d6f73e-95f0-4c4d-9b0f-489380c5187e

Public Version Date

September 08, 2020

Public Version Number

1

DI Record Publish Date

August 31, 2020

Package DI Number

20735471070316

Quantity per Package

20

Contains DI Package

10735471070319

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box